ibuprofen
- Product NDC
- 10267-3852
- 11-digit product format
- 102673852
- Labeler code
- 10267
- Product ID
- 10267-3852_77cf0092-7436-14ba-e053-2991aa0ac112
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ibuprofen
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Contract Pharmacal Corp.
- Application
- ANDA071265
- Marketing category
- ANDA
- Marketing start
- 2014-01-15
- Substance
- IBUPROFEN
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ibuprofen
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| IBUPROFEN | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | WK2XYI10QM |
| Rxcui | 310965 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10267-3852-2 | ibuprofen | 250 in 1 BOTTLE | TABLET | 250 | | 13 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10267-3852 | IBUPROFEN TABLET [CONTRACT PHARMACAL CORP.] | 13 | Current NDC, Legacy NDC, 1 package rows | 20181120_237bcb87-64a0-415b-bd53-e9d3b8bf33b6.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10267-3852-2 | 10267385202 | 250 TABLET in 1 BOTTLE (10267-3852-2) | 250 tablet | 2014-01-15 | 0000-00-00 | No | No | Current |